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KR900018028A - Improved process for preparing 3,5,6-trichloropyridin-2-ol - Google Patents

Improved process for preparing 3,5,6-trichloropyridin-2-ol Download PDF

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Publication number
KR900018028A
KR900018028A KR1019900006675A KR900006675A KR900018028A KR 900018028 A KR900018028 A KR 900018028A KR 1019900006675 A KR1019900006675 A KR 1019900006675A KR 900006675 A KR900006675 A KR 900006675A KR 900018028 A KR900018028 A KR 900018028A
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South Korea
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chloride
reacting
organic solvent
inert organic
hci
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KR1019900006675A
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KR0153446B1 (en
Inventor
가아쓰 퓨우스 알.
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리챠드 지. 워터맨
더 다우 케미칼 캄파니
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/19—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and carboxyl groups, other than cyano groups, bound to the same saturated acyclic carbon skeleton

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
  • Manufacture Of Tobacco Products (AREA)

Abstract

A process for the preparation of 3,5,6-trichloropyridin-2-ol from trichloroacetyl chloride and acrylonitrile is improved by separately conducting the individual addition, cyclization and aromatization steps. By separating these steps, water and HCl, which are by-products of the latter steps, can be precluded from interfering with the earlier steps. The individual process steps have also been improved.

Description

3,5,6-트리크로로피리딘-2-올의 개선된 제조 방법Improved process for preparing 3,5,6-trichloropyridin-2-ol

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (9)

환류 상태하에서 실시함으로써 형성된 특정의 HCI을 제거하면서, 촉매량의 구리 또는 제1구리염의 존재하에 50 내지 140℃의 온도에서 트리클로로아세틸 클로라이드를 아크릴로니트릴과 반응시킴을 포함하는, 2,2,4-트리클로로-4-시아노부타노일 클로라이드의 제조방법.2,2,4, comprising reacting trichloroacetyl chloride with acrylonitrile at a temperature of 50-140 ° C. in the presence of a catalytic amount of copper or cuprous salt, while removing certain HCI formed by carrying out under reflux. Method for preparing trichloro-4-cyanobutanoyl chloride. 제1항에 있어서, 대기압 내지 136 kPa이하의 약간 포지티브한(positive) 압력에서 수행하는 방법.The method of claim 1 wherein the process is carried out at a slightly positive pressure of atmospheric pressure up to 136 kPa. 136 내지 1.480kPa의 압력 및 주위온도 내지 100℃의 온도에서 불활성 유기용매중의 2,2,4-트리클로로-4-시아노부타노일 클로라이드와 무수 HCI을 반응시킴을 포함하는 3,3,5,6-테트라클로로-3,4-디하이드로피리딘-2-온의 제조 방법.3,3,5, comprising reacting anhydrous HCI with 2,2,4-trichloro-4-cyanobutanoyl chloride in an inert organic solvent at a pressure of from 136 to 1.480 kPa and from ambient to 100 ° C. Process for the preparation of 6-tetrachloro-3,4-dihydropyridin-2-one. 제3항에 있어서, 상기 불활성 유기용매가 방향족 탄화수소, 할로겐화 탄화수소 또는 카복실산 에스테르인 방법.4. The process of claim 3 wherein said inert organic solvent is an aromatic hydrocarbon, halogenated hydrocarbon or carboxylic acid ester. 불활성 유기용매중에서 3,3,5,6-테트라크로로-3,4-디하이드로피리딘-2-온을 클로라이드 이온과 반응시킴을 포함하는, 3,5,6-트리크로로피리딘-2-올의 개선된 제조 방법.3,5,6-trichloropyridine-2-, comprising reacting 3,3,5,6-tetrachloro-3,4-dihydropyridin-2-one with chloride ions in an inert organic solvent Improved Method of Making All. 제5항에 있어서, 상기 클로라이드 이온을, 디하이드로피리돈으로부터 HCI을 이탈시키는 것에 의해 동일 반응계에서 생성시키는 방법.The method according to claim 5, wherein the chloride ions are produced in situ by releasing HCI from dihydropyridone. 제5항에 또는 제6항에 있어서, 상기 불활성 유기용매가 방향족 탄화수소, 할로겐화 탄화수소 또는 카복실산에스테르인 방법.The method according to claim 5 or 6, wherein the inert organic solvent is an aromatic hydrocarbon, a halogenated hydrocarbon or a carboxylic acid ester. 제5항 내지 제7항중의 어느 한 항에 있어서, 상기 반응을 40 내지 120℃의 온도에서 수행하는 방법.The process according to claim 5, wherein the reaction is carried out at a temperature of 40 to 120 ° C. 9. (a)환류 상태하에서 실시함으로써 형성된 특정의 HCI를 제거하면서, 촉매량의 구리 또는 제1구리염의 존재하에 50 내지 140℃의 온도에서 트리클로로아세틸 클로라이들 아크릴로니트릴과 반응시켜 2,2,4-트리클로로-4-시아노부타노일 클로라이드를 생성시키는 단계;(b)136 내지 1.480kPa의 압력 및 주위돈도 내지 100℃의 온도에서 불활성 유기용매중의 2,2,4-트리클로로-4-시아노부타노일 클로라이드와 무수 HCI과 반응시켜 부타노일 클로라이드를 3,3,5,6-테트라크로로-3,4-디하이드로피리딘-2-온으로 고리화하는 단계; 및 (c)불활성 유기용매중에서 3,3,5,6-테트라크로로-3,4-디하이드로피리딘-2-온을 클로라이드 이온과 반응시켜 3,5,6-트로로피리딘-2-올을 생성시키는 단계를 포함하는, 3,5,6-트리클로로피리딘-2-올의 개선된 제조방법.(a) reacting with trichloroacetyl chloride acrylonitrile at a temperature of 50-140 ° C. in the presence of a catalytic amount of copper or cuprous salt while removing certain HCI formed by carrying out under reflux; Producing trichloro-4-cyanobutanoyl chloride; (b) 2,2,4-trichloro-4- in an inert organic solvent at a pressure of 136 to 1.480 kPa and a temperature of around 100 ° C. Reacting cyanobutanoyl chloride with anhydrous HCI to cyclize butanoyl chloride to 3,3,5,6-tetrachloro-3,4-dihydropyridin-2-one; And (c) reacting 3,3,5,6-tetrachloro-3,4-dihydropyridin-2-one with chloride ions in an inert organic solvent to give 3,5,6-troropyridin-2-ol. An improved method for preparing 3,5,6-trichloropyridin-2-ol, comprising the step of producing ※ 참고사항 : 최초출원내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019900006675A 1989-05-12 1990-05-11 An improved process for the preparation of 3.5.6-trichloropyridin-2-ol Expired - Fee Related KR0153446B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US350,961 1989-05-12
US07/350,961 US4996323A (en) 1989-05-12 1989-05-12 Process for the preparation of 3,5,6-trichloropyridin-2-ol

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KR900018028A true KR900018028A (en) 1990-12-20
KR0153446B1 KR0153446B1 (en) 1998-11-16

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US (1) US4996323A (en)
EP (1) EP0397281B1 (en)
JP (1) JP2829342B2 (en)
KR (1) KR0153446B1 (en)
CN (1) CN1027259C (en)
AT (1) ATE144979T1 (en)
AU (1) AU620245B2 (en)
BR (1) BR9001798A (en)
CA (1) CA2016620C (en)
DE (1) DE69029052T2 (en)
DK (1) DK0397281T3 (en)
ES (1) ES2095854T3 (en)
FI (1) FI97132C (en)
HU (2) HU913709D0 (en)
IL (1) IL94373A (en)
MX (1) MX166335B (en)
NZ (1) NZ233615A (en)
RU (1) RU1839671C (en)
UA (1) UA19168A1 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL86341A (en) * 1988-05-11 1992-02-16 Pamol Ltd Preparation of polychloropyridine derivatives and intermediates therefor
NL9000034A (en) * 1990-01-06 1991-08-01 Stamicarbon PROCESS FOR THE PREPARATION OF 5-OXOHEXANE NITRILLES AND THE SUBSTANCE 2,4-DIMETHYL-5-OXOHEXANE NITRILLES.
US5254712A (en) * 1990-01-06 1993-10-19 Stamicarbon B.V. Process for the preparation of 5-oxohexane nitriles and the compound 2,4-dimethyl-5-oxohexane nitrile
US5618942A (en) * 1993-09-03 1997-04-08 Luxembourg Industries (Pamol) Ltd. Production of 2,3,5,6-tetrachloropyridine
US5688953A (en) * 1996-07-31 1997-11-18 Dowelanco Process for the preparation of 3,3,5-trichloroglutarimide
CN102351785B (en) * 2011-08-11 2013-05-01 江苏九九久科技股份有限公司 Method for preparing 3, 5, 6-trichloropyridin-2-ol sodium
CN103086961A (en) * 2011-10-27 2013-05-08 山西三维丰海化工有限公司 Method for producing pyridone from chloroacetic acid waste liquid
CN103086959A (en) * 2011-10-27 2013-05-08 山西三维丰海化工有限公司 Novel process for producing 3,5,6-sodium trichloropyrindinol
CN103086960A (en) * 2011-10-27 2013-05-08 山西康得利精细化工有限公司 Novel process for producing chlopyrifos from pyridone by using aqueous phase method
CN103193705A (en) * 2013-03-22 2013-07-10 浙江工业大学 Synthesis method of 2-chloronicotinic acid and derivative thereof
CN103274996B (en) * 2013-05-02 2015-08-19 江苏九九久科技股份有限公司 The one kettle way of improvement prepares the method for 3,5,6-trichloropyridine-2-sodium alkoxide
CN103819397B (en) * 2014-03-14 2015-12-30 杨雪飞 A kind of efficient catalytic synthetic method of heterocyclic alcohol
CN104876858A (en) * 2015-05-13 2015-09-02 安徽国星生物化学有限公司 One-pot method for synthesizing sodium 3,5,6-trichloropyridin-2-olate

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3007931A (en) * 1959-03-09 1961-11-07 Phillips Petroleum Co Production of unsaturated heterocyclic nitrogen bases
US4245098A (en) * 1978-12-05 1981-01-13 Ciba-Geigy Corporation Process for producing 2,3,5-trichloropyridine, 2,4,4-trichloro-4-formyl-butyronitrile as a novel compound and a process for producing it
EP0030214B1 (en) * 1979-11-30 1985-01-30 Ciba-Geigy Ag Process for the preparation of 2,3,5,6-tetrachloropyridine and 3,5,6-trichloropyridin-2-ol
US4469896A (en) * 1981-08-17 1984-09-04 Ciba-Geigy Corporation Process for the production of chloropyridines substituted by methyl, trichloromethyl or trifluoromethyl groups
US4435573A (en) * 1982-10-25 1984-03-06 The Dow Chemical Company Process for the preparation of substituted pyridines
US4468354A (en) * 1983-02-15 1984-08-28 The Dow Chemical Company Continuous process for preparing 5-oxo-2,4-dichloro-4-substituted pentanenitriles
US4465186A (en) * 1983-07-14 1984-08-14 Meyers Jonathan H Holder for clips
AR243869A1 (en) * 1987-06-05 1993-09-30 Quimica Estrella Aca Sa A procedure for synthesising 2-hydroxy-3,5,6-trichloropyridine.
JPS63313771A (en) * 1987-06-15 1988-12-21 Nippon Kayaku Co Ltd Production of 3,5,6-trichloro-2-pyridinol
IL86341A (en) * 1988-05-11 1992-02-16 Pamol Ltd Preparation of polychloropyridine derivatives and intermediates therefor

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Publication number Publication date
AU5494590A (en) 1990-11-15
RU1839671C (en) 1993-12-30
DE69029052D1 (en) 1996-12-12
HU205078B (en) 1992-03-30
JPH035458A (en) 1991-01-11
EP0397281B1 (en) 1996-11-06
MX166335B (en) 1992-12-29
BR9001798A (en) 1991-06-11
CA2016620C (en) 2001-05-08
KR0153446B1 (en) 1998-11-16
HU903008D0 (en) 1990-09-28
EP0397281A2 (en) 1990-11-14
ATE144979T1 (en) 1996-11-15
HU913709D0 (en) 1992-02-28
FI97132B (en) 1996-07-15
JP2829342B2 (en) 1998-11-25
FI97132C (en) 1996-10-25
IL94373A0 (en) 1991-03-10
FI902363A0 (en) 1990-05-11
CN1047281A (en) 1990-11-28
DE69029052T2 (en) 1997-03-06
CN1027259C (en) 1995-01-04
ES2095854T3 (en) 1997-03-01
EP0397281A3 (en) 1991-10-02
IL94373A (en) 1994-06-24
UA19168A1 (en) 1997-12-25
CA2016620A1 (en) 1990-11-12
US4996323A (en) 1991-02-26
AU620245B2 (en) 1992-02-13
DK0397281T3 (en) 1997-04-14
NZ233615A (en) 1992-06-25
HUT54984A (en) 1991-04-29

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St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000